S. M. Kim

Distal hereditary motor neuropathy type 7B with Dynactin 1 mutation.

Byung-Ok Choi, Y. Hong, K. Chung, 2016, Molecular medicine reports.

A Mutation in PMP2 Causes Dominant Demyelinating Charcot-Marie-Tooth Neuropathy

H. Koo, G. Kwak, Won Min Mo, 2016, PLoS genetics.

Identification of Korean-specific SNP markers from whole-exome sequencing data

K. Chung, S. Yoo, S. H. Nam, 2016, International Journal of Legal Medicine.

Severe phenotypes in a Charcot–Marie–Tooth 1A patient with PMP22 triplication

Byung-Ok Choi, K. Chung, Jinho Lee, 2014, Journal of Human Genetics.

X‐linked Charcot‐Marie‐Tooth disease type 6 (CMTX6) patients with a p.R158H mutation in the pyruvate dehydrogenase kinase isoenzyme 3 gene

Byung-Ok Choi, Y. Hong, Anna H. Siddell, 2016, Journal of the peripheral nervous system : JPNS.